Method for modulating, regulating and/or stabilizing angiogenesis

ABSTRACT

A method of modulating, regulating and/or stabilizing angiogenesis in a mammal in need thereof, in which the PDGF-D level or activity or both in the mammal are modulated or increased. In preferred embodiments, an active PDGF-D polypeptide, or a polynucleotide encoding an active PDGF-D is administered to the mammal, preferably at a location where angiogenesis modulation or stabilization is desired. The PDGF-D is advantageously co-administered with an angiogenic growth factor, such as a member of the VEGF family of growth factors, in particular VEGF-E. The claimed method inhibits leakage of blood vessels and is useful, inter alia, for treatment of edemas.

CROSS-REFERENCES TO RELATED APPLICATIONS

This application is a divisional of application Ser. No. 11/073,605, filed Mar. 8, 2005, which claims priority of U.S. Provisional Application Ser. No. 60/550,327, filed Mar. 8, 2004, the content of which are incorporated herein by reference in their entireties.

FIELD OF THE INVENTION

This invention relates to the use of PDGF-D to modulate, regulate and/or stabilize angiogenesis, especially angiogenesis induced by angiogenic growth factors such as the various members of the VEGF family of growth factors, particularly VEGF-E.

BACKGROUND OF THE INVENTION

In the developing embryo, the primary vascular network is established by in situ differentiation of mesodermal cells in a process called vasculogenesis. It is believed that all subsequent processes involving the generation of new vessels in the embryo and neovascularization in adults, are governed by the sprouting or splitting of new capillaries from the pre-existing vasculature in a process called angiogenesis (Pepper et al., 1996, Enzyme & Protein, 49:38-162; Breier et al., 1995, Dev. Dyn., 204:228-239; Risau, 1997, Nature, 386:671-674). Angiogenesis is not only involved in embryonic development and normal tissue growth, repair, and regeneration, but is also involved in the female reproductive cycle, establishment and maintenance of pregnancy, and in repair of wounds and fractures. In addition to angiogenesis which takes place in the normal individual, angiogenic events are involved in a number of pathological processes, notably tumor growth and metastasis, and other conditions in which blood vessel proliferation, especially of the microvascular system, is increased, such as diabetic retinopathy, psoriasis and arthropathies. Modulation, regulation and/or stabilization of angiogenesis is useful in preventing or alleviating various pathological processes.

On the other hand, promotion of angiogenesis is desirable in situations where vascularization is to be established or extended, for example after tissue or organ transplantation, or to stimulate establishment of collateral circulation in tissue infarction or arterial stenosis, such as in coronary heart disease and thromboangiitis obliterans.

The angiogenic process is highly complex and involves the maintenance of the endothelial cells in the cell cycle, degradation of the extracellular matrix, migration and invasion of the surrounding tissue and finally, tube formation. The molecular mechanisms underlying the complex angiogenic processes are far from being understood.

Because of the crucial role of angiogenesis in so many physiological and pathological processes, factors involved in the control of angiogenesis have been intensively investigated. A number of growth factors have been shown to be involved in the regulation of angiogenesis; these include fibroblast growth factors (FGFs), platelet-derived growth factor (PDGF), transforming growth factor alpha (TGFα), and hepatocyte growth factor (HGF). See for example Folkman et al., 1992, J. Biol. Chem., 267:10931-10934 for a review.

It has been suggested that a particular family of endothelial cell specific growth factors, the vascular endothelial growth factors (VEGFs), and their corresponding receptors are primarily responsible for stimulation of endothelial cell growth and differentiation, and for certain functions of the differentiated cells. These factors are members of the PDGF family, and appear to act primarily via endothelial receptor tyrosine kinases (RTKs).

The VEGF family members share a VEGF homology domain which contains the six cysteine residues which form the cysteine knot motif. Functional characteristics of the VEGF family include varying degrees of mitogenicity for endothelial cells, induction of vascular permeability and angiogenic and lymphangiogenic properties.

Similarity between two proteins is determined by comparing the amino acid sequence and conserved amino acid substitutions of one of the proteins to the sequence of the second protein, whereas identity is determined without including the conserved amino acid substitutions.

PDGF/VEGF family members act primarily by binding to receptor tyrosine kinases. Five endothelial cell-specific receptor tyrosine kinases have been identified, namely VEGFR-1 (FIt-I), VEGFR-2 (KDR/Flk-1), VEGFR-3 (Flt4), Tie and Tek/Tie-2. All of these have the intrinsic tyrosine kinase activity which is necessary for signal transduction. The essential, specific role in vasculogenesis and angiogenesis of VEGFR-1, VEGFR-2, VEGFR-3, Tie and Tek/Tie-2 has been demonstrated by targeted mutations inactivating these receptors in mouse embryos.

The only receptor tyrosine kinases known to bind VEGFs are VEGFR-1, VEGFR-2 and VEGFR-3. VEGFR-1 and VEGFR-2 bind VEGF with high affinity, and VEGFR-1 also binds VEGF-B and PIGF. VEGF-C has been shown to be the ligand for YEGFR-3, and it also activates VEGFR-2 (Joukov et al., 1996, The EMBO Journal, 15:290-298). VEGF-D binds to both VEGFR-2 and VEGFR-3. VEGF-E binds with high affinity to VEGFR-2 and neuropilin-1, but neither to VEGFR-1 nor to VEGFR-3, inducing vascular permeability and potent angiogenic activity both in vitro and in vivo (Ogawa et al., J. Biol. Chem. 1998. 273: 31273-31282; Meyer et al., EMBO J. 1999. 18: 363 374; Wise et al., Proc. Natl. Acad. Sci. USA 1999. 96: 3071-3076.). A ligand for Tek/Tie-2 has been described in International Patent Application No. PCT/US95/12935 (WO 96/11269) by Regeneron Pharmaceuticals, Inc. The ligand for Tie has not yet been identified.

The isolation and cloning of a novel 130-135 kDa VEGF isoform specific receptor has been reported in Soker et al., 1998, Cell, 92:735-745. This VEGF receptor was found to specifically bind the VEGF165 isoform via the exon 7 encoded sequence, which shows weak affinity for heparin (Soker et al., 1998, Cell, 92:735-745). Surprisingly, the receptor was shown to be identical to human neuropilin-1 (NP-1), a receptor involved in early stage neuromorphogenesis. PIGF-2 also appears to interact with NP-1 (Migdal et al., 1998, J. Biol. Chem., 273:22272-22278).

VEGFR-1, VEGFR-2 and VEGFR-3 are expressed differently by endothelial cells. Both VEGFR-I and VEGFR-2 are expressed in blood vessel endothelia (Oelrichs et al., 1992, Oncogene, 8:11-18; Kaipainen et al., 1993, J. Exp. Med., 178:2077-2088; Dumont et al., 1995, Dev. Dyn., 203:80-92; Fong et al., 1996, Dev. Dyn., 207: 1-10) and VEGFR-3 is mostly expressed in the lymphatic endothelium of adult tissues (Kaipainen et al., 1995, Proc. Natl. Acad. Sci. USA, 9:3566-3570). VEGFR-3 is also expressed in the blood vasculature surrounding tumors.

Disruption of the VEGFR genes results in aberrant development of the vasculature leading to embryonic lethality around midgestation. Analysis of embryos carrying a completely inactivated VEGFR-I gene suggests that this receptor is required for functional organization of the endothelium (Fong et al., 1995, Nature, 376:66-70). However, deletion of the intracellular tyrosine kinase domain of VEGFR-I generates viable mice with a normal vasculature (Hiratsuka et al., 1998, Proc. Natl. Acad. Sci. USA, 95:9349-9354). The reasons underlying these differences remain to be explained but suggest that receptor signaling via the tyrosine kinase is not required for the proper function of VEGFR-1. Analysis of homozygous mice with inactivated alleles of VEGFR-2 suggests that this receptor is required for endothelial cell proliferation, hematopoiesis and vasculogenesis (Shalaby et al., 1995, Nature, 376:62-66; Shalaby et al., 1997, Cell, 89:981-990). Inactivation of VEGFR-3 results in cardiovascular failure due to abnormal organization of the large vessels (Dumont et al., 1998, Science, 282:946-949).

Although VEGFR-I is mainly expressed in endothelial cells during development, it can also be found in hematopoetic precursor cells during early stages of embryogenesis (Fong et al., 1995, Nature, 376:66-70). It is also is expressed by most, if not all, vessels in embryos (Breier et al., 1995, Dev. Dyn., 204:228-239; Fong et al., 1996, Dev. Dyn., 207:1-10). In adults, monocytes and macrophages also express this receptor (Barleon et al., 1996, Blood, 87:33363343).

The receptor VEGFR-3 is widely expressed on endothelial cells during early embryonic development, but as embryogenesis proceeds, it becomes restricted to venous endothelium and then to the lymphatic endothelium (Kaipainen et al., 1994, Cancer Res., 54:6571-6577; Kaipainen et al., 1995, Proc. Natl. Acad. Sci. USA, 92:3566-3570). VEGFR-3 continues to be expressed on lymphatic endothelial cells in adults. This receptor is essential for vascular development during embryogenesis. Targeted inactivation of both copies of the VEGFR-3 gene in mice resulted in defective blood vessel formation characterized by abnormally organized large vessels with defective lumens, leading to fluid accumulation in the pericardial cavity and cardiovascular failure at post-coital day 9.5. On the basis of these findings it has been proposed that VEGFR-3 is required for the maturation of primary vascular networks into larger blood vessels. However, the role of VEGFR-3 in the development of the lymphatic vasculature could not be studied in these mice because the embryos died before the lymphatic system emerged. Nevertheless it is assumed that VEGFR-3 plays a role in development of the lymphatic vasculature and lymphangiogenesis given its specific expression in lymphatic endothelial cells during embryogenesis and adult life. This is supported by the finding that ectopic expression of VEGF-C, a ligand for VEGFR-3, in the skin of transgenic mice, resulted in lymphatic endothelial cell proliferation and vessel enlargement in the dermis. Furthermore this suggests that VEGF-C may have a primary function in lymphatic endothelium, and a secondary function in angiogenesis and permeability regulation which is shared with VEGF (Joukov et al., 1996, EMBO J., 15:290-298).

PDGF plays an important role in the growth and/or motility of connective tissue cells, fibroblasts, myofibroblasts and glial cells (Heldin et al., “Structure of platelet-derived growth factor: Implications for functional properties”, 1993, Growth Factor, 8:245-252). In adults, PDGF stimulates wound healing (Robson et al., 1992, Lancet, 339:23-25). Structurally, PDGF isoforms are disulfide-bonded dimers of homologous A- and B-polypeptide chains, arranged as homodimers (PDGF-AA and PDGF-BB) or a heterodimer (PDGFAB).

PDGF isoforms exert their effects on target cells by binding to two structurally related receptor tyrosine kinases (RTKs). The alpha-receptor binds both the A- and B-chains of PDGF, whereas the beta-receptor binds only the B-chain. These two receptors are expressed by many cell lines grown in vitro, and are mainly expressed by mesenchymal cells in vivo. The PDGFs regulate cell proliferation, cell survival and chemotaxis of many cell types in vitro (reviewed in Heldin et al., 1998, Biochim. Biophys. Acta, 1378:F79-113). In vivo, they exert their effects in a paracrine mode since they often are expressed in epithelial (PDGF-A) or endothelial cells (PDGF-B) in close apposition to the PDGFR expressing mesenchyme. In tumor cells and in cell lines grown in vitro, coexpression of the PDGFs and the receptors generate autocrine loops which are important for cellular transformation (Betsholtz et al., 1984, Cell, 39:447-57; Keating et al., 1990, J. R. Coll Surg Edinb., 35:172-4). Overexpression of the PDGFs have been observe in several pathological conditions, including malignancies, arteriosclerosis, and fibroproliferative diseases (reviewed in Heldin et al., 1996, The Molecular and Cellular Biology of Wound Repair, New York: Plenum Press, 249-273).

The importance of the PDGFs as regulators of cell proliferation and survival are well illustrated by recent gene targeting studies in mice that have shown distinct physiological roles for the PDGFs and their receptors despite the overlapping ligand specificities of the PDGFRs. Homozygous null mutations for either of the two PDGF ligands or the receptors are lethal. Approximately 50% of the homozygous PDGF-A deficient mice have an early lethal phenotype, while the surviving animals have a complex postnatal phenotype with lung emphysema due to improper alveolar septum formation because of a lack of alveolar myofibroblasts (Boström et al., 1996, Cell, 85:863-873). The PDGF-A deficient mice also have a dermal phenotype characterized by thin dermis, misshapen hair follicles and thin hair (Karlsson et al., 1999, Development, 126:2611-2). PDGF-A is also required for normal development of oligodendrocytes and subsequent myelination of the central nervous system (Fruttiger et al., 1999, Development, 126:457-67). The phenotype of PDGFR-alpha deficient mice is more severe with early embryonic death at E10, incomplete cephalic closure, impaired neural crest development, cardiovascular defects, skeletal defects, and edemas (Soriano et al., 1997, Development, 124:2691-70). The PDGF-B and PDGFR-beta deficient mice develop similar phenotypes that are characterized by renal, hematological and cardiovascular abnormalities (Levéen et al., 1994, Genes Dev., 8:1875-1887; Soriano et al., 1994, Genes Dev., 8:1888-96; Lindahl et al., 1997, Science, 277:242-5; Lindahl, 1998, Development, 125:3313-2), where the renal and cardiovascular defects, at least in part, are due to the lack of proper recruitment of mural cells (vascular smooth muscle cells, pericytes or mesangial cells) to blood vessels (Levéen et al., 1994, Genes Dev., 8:1875-1887; Lindahl et al., 1997, Science, 277:242-5; Lindahl et al., 1998, Development, 125:3313-2).

A member of the PDGF family of growth factors is PDGF-D, which is described in International patent application no. WO 00/27879 and published US application no. 2002/0164710 AI, the entire contents of which are incorporated herein by reference. PDGF-D has the ability to stimulate, or enhance, or both, one or more of proliferation, differentiation, growth, and motility of cells expressing a PDGF-D receptor. Cells affected by PDGF-D include, but are not limited to, endothelial cells, connective tissue cells, myofibroblasts and glial cells. PDGF-D and compositions containing it are useful for various therapeutic applications involving the modulation, regulation and/or stabilization of angiogenesis, and particularly for the treatment of edemas which result from leaky vessels.

PDGF-D is structurally homologous to PDGF-A, PDGF-B, VEGF, VEGF-B, VEGF-C and VEGF-D. The polynucleotide sequence of at least nucleotides 935 to 1285 set out in FIG. 2 (SEQ ID NO: 1) encodes a portion of the PDGF/VEGF homology domain, which is the bioactive fragment of PDGF-D. The bioactive fragment is also included in the 200 amino acids set out in FIG. 3 (SEQ ID NO:3) (excluding the first 24 amino acid residues, which are due to a cloning artifact) or the 322 amino acid sequence set out in FIG. 4 (SEQ ID NO:4).

PDGF-D has the ability to stimulate one or more of proliferation, differentiation, motility, survival or vascular permeability of cells expressing a PDGF-D receptor including, but not limited to, vascular endothelial cells, lymphatic endothelial cells, connective tissue cells (such as fibroblasts), myofibroblasts and glial cells. PDGF-D also has the ability to stimulate wound healing. A preferred fragment is a truncated form of PDGF-D comprising a portion of the PDGF/VEGF homology domain (PVHD) of PDGF-D. The portion of the PVHD is from residues 254-370 of FIG. 1 (SEQ ID NO: 2) where the putative proteolytic processing site RKSK starts at amino acid residue 254 (SEQ ID NO: 2). However, the PVHD extends toward the N terminus up to residue 234 of FIG. 1 (SEQ ID NO: 2). Herein the PVHD is defined as truncated PDGF-D. The truncated PDGF-D is the putative activated form of PDGF-D.

As indicated above, there are numerous clinical situations where angiogenesis is desired to be promoted, and methods have been proposed using one of the numerous members of the VEGF/PDGF family of growth factors known to have angiogenesis stimulation effects. For example, VEGF has been shown to be intimately involved in the entire sequence of events leading to growth of new blood vessels. Gross et al., Proc. Nat'l. Acad. Sci., 80(9): 2623-27 (1983), Folkman et al., Proc. Nat'l. Acad. Sci., 76(10): 5217-21 (1979). Five human VEGF isoforms of 121, 145, 165, 189 and 206 amino acids have been isolated. Gross, et al., Proc. Nat'l. Acad. Sci., 80(9): 2623-27 (1983), Leung, et al., Science, 246: 1306-09 (1989), Poltorak et al., J. Biol. Chem., 272(11): 7151-78 (1997). Among the isoforms, VEGF 165 seems to be the most effective and most commonly used. The effect of VEGF 165 in augmenting perfusion and in stimulating formation of collateral vessels has been shown in animal models Hopkins et al., J. Vascular Surgery, 27(5): 886-94 (1998), Asahara et al., Circulation, 91(11): 2793-801 (1995), Hariawala et al., J. Surg. Res., 63(1): 77-82 (1996), Bauters et al., Circulation, 91(11): 2802-9 (1995), Bauters et al., Am. J. Physiol., 267(4 Pt 2): H1263-71 (1994), Takeshita et al., J. Clin. Invest., 93(2):662-70 (1994), Takeshita, et al., Circulation, 90(5 Pt 2): 11228-34 (1994), Takeshita, et al., Am. J. Path., 147(6): 1649-60 (1995), Banai, et al., Circulation, 89(5): 2183-9 (1994). In clinical trials, successful induction of collateral blood vessels in ischemic heart disease and critical limb ischemia by VEGF have also been reported. Baumgartner et al., Circulation, 97(12): 1114-23 (1998), Losordo, et al., Am. Heart J., 138(2 Pt 2): 132-41 (1999).

Angiogenesis, however, is a complex process that includes activation, migration and proliferation of endothelial cells and formation of new blood vessels. D'Amore, et al., Ann. Rev. Physiol., 49(9-10): 453-64 (1987). The process likely requires a network of members of the VEGF/PDGF family of growth factors, and use of a single factor alone in promoting angiogenesis may have undesired or unsatisfactory results. For example, it is known that the vascular endothelial growth factor-A (“VEGF”) causes both abnormal blood vessel growth (angiogenesis) and blood vessel leakage in the eye. Specifically, preclinical studies have shown that a) in multiple animal species, including humans, VEGF levels are elevated around growing and leaky blood vessels, b) blocking VEGF results in the prevention and regression of these abnormal vessels in primates and other species and c) VEGF alone is sufficient to trigger the abnormal blood vessel growth and blood vessel leakage that characterizes wet age-related macular degeneration (AMD). See A. P. Adamis et al., Inhibition of vascular endothelial growth factor prevents retinal ischemia-associated iris neovascularization in a nonhuman primate, 114(1) Arch. Opthalmol. 66-71 (1996); A. Kvanta et al., Subfoveal fibrovascular membranes in age-related macular degeneration express vascular endothelial growth factor, 37 Invest. Opthalmol. Vis. Sci. 1929-34 (1996); G. Lutty et al., Localization of VEGF in human retina and choroids, 114 Arch. Opthalmol. 971-77 (1996); M. J. Tolentino et al., Intravitreous injections of vascular endothelial growth factor produce retinal ischemia and microangiopathy in an adult primate, 103(11), Opthalmology 1820-28 (1996); M. J. Tolentino, Vascular endothelial growth factor is sufficient to produce iris neovascularization and neovascular glaucoma in a nonhuman primate, 114(8) Arch. Ophthalmol. 964-70 (1996). To minimize the undesired effect of VEGF, VEGF antagonists have been proposed, but these antagonists are obviously not suitable for situations where stimulation of angiogenesis is desired.

Thus, there IS a significant need to be able to modulate the angiogenesis promoting activities of one member of the PDGF/VEGF family of growth factors, preferably with another member of the family.

SUMMARY OF THE INVENTION

It has now been found that PDGF-D can act to modulate, regulate and/or stabilize angiogenesis.

In particular, it has been found that PDGF-D can act to stabilize the vessels induced by angiogenic activity of other angiogenic growth factors, such as members of the VEGF family of growth factors, particularly VEGF-E.

According to the present invention, any polypeptide sequence having a VEGF-E activity is suitable. For example, VEGF-E derivatives, variants and analogs are suitable and include polypeptides that are at least 70% or at least 80% identical to SEQ ID NO: 15 (FIG. 8). In this regard, polypeptides at least 90% identical to the same are particularly preferred, and among these particularly preferred polynucleotides, those with at least 95% are especially preferred. Furthermore, those with at least 97% are highly preferred among those with at least 95%, and among these those with at least 98% and at least 99% are particularly highly preferred, with at least 99% being the more preferred.

It has additionally been found that PDGF-D can act to reduce the leakage of leaky vessels, by for example inducing or stimulating the proliferation and migration of smooth muscle cells (SMC).

Another aspect of the invention provides for the use of vectors comprising PDGF-D DNA and host cells transformed or transfected with nucleic acid molecules or vectors of the invention. These may be eukaryotic or prokaryotic in origin. These cells are particularly suitable for expression of the polypeptide of the invention, and include insect cells such as Sf9 cells, obtainable from the American Type Culture Collection (ATCC SRL-171), transformed with a baculovirus vector, and the human embryo kidney cell line 293-EBNA transfected by a suitable expression plasmid. Preferred vectors of the invention are expression vectors in which a nucleic acid according to the invention is operatively connected to one or more appropriate promoters and/or other control sequences, such that appropriate host cells transformed or transfected with the vectors are capable of expressing the polypeptide of the invention. Other preferred vectors are those suitable for transfection of mammalian cells, or for gene therapy, such as adenoviral-, adeno-associated virus, vaccinia- or retroviral based vectors or liposomes. A variety of such vectors is known in the art. These vectors may be used to generate PDGF-D in situ to modulate, regulate and/or stabilize angiogenic activity.

Clinical applications of the invention include stabilization of angiogenesis in tissue or organ transplantation to promote graft growth and vascularization, or in wound healing, or in connective tissue development, or in the establishment of collateral circulation in tissue infarction or arterial stenosis, such as coronary artery disease.

The angiogenesis-modulating and/or stabilizing effects of PDGF-D may also be relevant to a variety of lung conditions. PDGF-D could be used in the treatment of lung disorders to improve blood circulation in the lung and/or gaseous exchange between the lungs and the blood stream. Similarly, PDGF-D could be used to improve blood circulation to the heart and 02 gas permeability in cases of cardiac insufficiency. In a like manner, PDGF-D could be used to improve blood flow and gaseous exchange in chronic obstructive airway diseases.

Thus the invention provides a method for stabilizing, regulating or modulating angiogenesis, lymphangiogenesis, neovascularization, connective tissue development and/or wound healing in a mammal in need of such treatment, comprising the step of administering an effective dose of PDGF-D, or a fragment or an analog thereof which has the biological activity of PDGF-D to the mammal. The PDGF-D polypeptides may be administered either in the form of its bioactive fragment (e.g. residues 254-370 of SEQ ID NO:2), or in the form of a full-length sequence which may be activated, e.g. with a suitable protease, in situ. Alternatively, a nucleic acid molecule coding for a bioactive PDGF-D polypeptide may be administered, or a nucleic acid molecule coding for a full length PDGF-D polypeptide together with a nucleic acid molecule coding for a suitable protease are administered together, preferably under the control of regulatory elements suitable for regulation of their respective expression. Optionally the PDGF-D, or fragment or analog thereof may be administered together with, or in conjunction with, one or more of VEGF, VEGF-B, VEGF-C, VEGF-D, PIGF, PDGF-A, PDGF-B, PDGF-C, FGF and/or heparin.

PDGF-D polypeptides may be directly delivered to the site of interest where angiogenesis etc are desired. Numerous direct polypeptide delivery methods are known and may be used. See e.g. Talmadge, 1993, The pharmaceutics and delivery of therapeutic polypeptides and proteins, Adv. Drug Del. Rev. 10:247-299. The polypeptides may be administered orally. Although polypeptides are generally known to have poor availability through oral administration, various methods known in the art have been developed to overcome this limitation. For example, biodegradable polymeric matrices have been used for delivering proteins over a desired period of time. For example, the use of biodegradable poly(d, l-lactic-co-glycolic acid) (PLGA) microspheres for the delivery of peptides and proteins has been widely reported (Mehta et al., 1996, Peptide containing microspheres from low molecular weight and hydrophilic poly(d,l-lactide-co-glycolide), J. Control Release 41:249-257; Chiba et al., 1997, Controlled protein delivery from biodegradable tyrosine-containing poly(anhydride-co-imide) microspheres. Biomaterials 18:893-901; Ravivarapu et al., 2000, Polymer and microsphere blending to alter the release of a peptide from PLGA microspheres, Eur. J. Pharm. Biopharm. 50:263-270).

Preferably, direct application of the polypeptides, especially direct injection, or topical application, may be used. Because wound-healing and other conditions requiring enhanced angiogenesis typically require local application of PDGF-D polypeptides and other growth factors for only a limited time, direct injection, even frequent direct injection of the polypeptides to the desired site(s) is acceptable and is not likely to be very tedious or expensive and pose problems such as poor patient acceptance. Methods of direct application of polypeptides are well-known to those ordinarily skilled in the art, and recent successes, strategies, and potentials of topical application of PDGF-BB in improving healing were reviewed by Cupp et al., 2002, Gene therapy, electroporation, and the future of wound-healing therapies, Facial Plast. Burg. 18:53-57.

In another preferred embodiment, the therapeutic polypeptides of the present invention may be delivered in the form of nucleic acid molecules encoding the polypeptides. Many established and well-known methods for gene delivery or gene therapy may be used for administering genes or other nucleic acid molecules encoding PDGF-D to the patient. Bee e.g. Rubany, 2001, The future of human gene therapy, Mol. Aspects. Med. 22:113-42. A single dose of naked DNA of VEGF and PDGF was used to treat rats with cysteamine-induced duodenal ulcers, and was shown to significantly accelerate chronic duodenal ulcer healing, and increase VEGF and PDGF levels in duodenal mucosa (Szabo et al., 2001, Gene Expression and gene therapy in experimental duodena ulceration, J. Physiol. Paris 95:325-335).

The polynucleotides encoding PDGF-D preferably are linked operatively under the control of suitable promoter so that they are expressed when taken up by the host cells. PDGF-D is a diffusible protein, and as such it will exert its effects on cells directly expressing the polypeptides, as well as on surrounding cells. Accordingly, suitable promoters may be constitutive promoters such as promoter and enhancer elements from cytomegalovirus (CMV), Rous sarcoma virus (RSV), and SV40, and the rat beta-actin promoter. Preferably, inducible or tissue specific promoters are used to increase expression level, improve specificity and reduce side effects. In this regard, suitable promoters include the keratin 5 (K5) promoter (Pierce et al., 1998, Oncogene 16: 1267-1276; Pierce et al., 1998, Proc. Natl. Acad. Sci. USA 95:8858-8863), the Cyr61 promoter (inducible in granulation tissue during wound healing) (Latinkic et al., 2001, Promoter function of the angiogenic inducer Cyr61 gene in transgenic mice: tissue specificity, inducibility during wound healing, and role of the serum response element, Endocrinol. 142:2549-2557), and the FAP promoter (Neidermeyer et al., 2001, Expression of the fibroblast activation protein during mouse embryo development, Int. J. Dev. Biol. 45:445-447).

Suitable polynucleotides may also be delivered as nonviral vectors, using methods well-known to those ordinarily skilled in the art. See e.g. Brown et al., 2001, Gene delivery with synthetic (non-viral) carriers, Int. J. Pharm. 229:1-21; and Pouton et al., 1998, Key issues in non-viral gene delivery, Adv. Drug Deliv. Rev. 34:3-19.). Lipofection, liposome mediated gene transfer are preferred (Romano et al., 1999, Gene transfer technology in therapy: current applications and future goals. Stem Cells 17:191-202; Mountain, 2000, Gene therapy: the first decade. Trends. Biotechnol. 18:119-28; Mhashilkar et al., 2001, Gene therapy: Therapeutic approaches and implications. Biotechnol. Adv. 19:279-97; and Lasic, 1998, Novel applications of liposomes, Trends Biotechnol. 16:307-21).

One of the simplest ideas for non-viral gene delivery is the use of purified DNA in the form of plasmids. A naked polynucleotide operatively coding for the polypeptide may be delivered, along with a pharmaceutically acceptable carrier, directly to the desired site, where the polynucleotide is taken up by the cells at the site and expressed or otherwise exerts its therapeutic effects. This is particularly preferred if transient expression of the gene is desired. The transfer of naked DNA by physical means is well known, by such means as gene guns and electroporation. See e.g. Spack et al., 2001, Developing non-viral DNA delivery systems for cancer and infectious disease, DDT 6:186-97. See also Cupp et al., 2002, supra.

In general, RNA molecules will have more transient effects than DNA molecules. The effects of the naked RNA molecules so delivered last typically for less than about 20 days, usually less than 10 days, and often less than 3 to 5 days. Delivery may be by injection, spray, biolistic methods, and so on, depending on the site.

In another embodiment, suitable polynucleotides may also be delivered within viral vectors, which are known to have higher transfection efficiency compared to nonviral vectors. See e.g. Robbins et al., 1998, Viral vectors for gene therapy, Pharmacol. Ther. 80:35-47; and Kay et al., 2001, Viral vectors for gene therapy: the art of turning infectious agents into vehicles of therapeutics, Nat. Med. 7:33-40. Suitable viral vectors include those derived from retroviruses (including lentivirues) (see e.g. Breithart et al., 1999, Ann. Plast. Surg. 43:632-9), especially the Moloney murine leukemia virus and pseudotyped retroviruses (Chen et al., 2001, Safety testing for replication competent retrovirus associated with gibbon ape leukemia virus-pseudotyped retroviral vectors. Hum. Gene. Ther. 12:61-70); adenoviruses, especially the third generation “gutless” adenoviral vector (Kochanek et al., 2001, High-capacity “gutless” adenoviral vectors. Curr. Opin. Mol. Ther. 3:454-63.); chimeric viruses that combine the advantages of both retroviruses and adenoviruses (Reynolds et al., 1999, Chimeric viral vectors—the best of both worlds? Mol. Med. Today 5:25-31, 1999); adeno-associated virus (Ponnazhagan et al., 2001, Adeno-associated virus for gene therapy. Cancer Res., 61:6313-21; and Monahan et al., 2000, Adeno-associated virus vectors for gene therapy: more pros than cons? Mol. Med. Today, 6:433-40.); vaccinia viruses (Peplinski, et al., 1998, Vaccinia virus for human gene therapy. Surg. Oncol. Clin. N. Am., 7:575-588); and herpes simplex virus (Latchman. 2001, Gene delivery and gene therapy with herpes simplex virus-based vectors. Gene 264:1-9).

Adenoviral vectors are preferred. Chen et al. (2002) showed that recombinant adenoviruses encoding the PDGF-A gene express and secrete PDGF-A in vitro, and induce sustained down regulation of PDGFaR encoded by the growth arrest specific (gas) gene (Am. J. Physiol. Cell Physiol. 282:C538-44). Szabo et al., supra, used a single dose of adenoviral vectors expressing VEGF and PDGF to treat rats with cysteamine-induced duodenal ulcers, and showed significant acceleration of chronic duodenal ulcer healing, and increased VEGF and PDGF levels in duodenal mucosa. Giannobile et al., 2001, J. Periodontol. 72:815-23 showed that adenoviral vectors expressing PDGF-A stimulated cementoblast DNA synthesis and subsequent proliferation. Zhu et al., 2001, J. Dent. Res. 80:892-7 demonstrated that adenoviruses encoding PDGF-A enhanced mitogenic and proliferative responses in osteoblasts, periodontal ligament fibroblasts and gingival fibroblasts. See also Liechty et al., 1999, Adenoviral mediated overexpression of PDGF-B corrects ischemic impaired wound healing, J. Invest. Dermatol. 113:375-83.

The effects of vectors coding for PDGF-D polypeptides may also be improved with matrix immobilization to enhance tissue repair activity. Biocompatible matrices capable of immobilizing adenoviral vectors have been successfully used in treating ischemic excisional wounds. Specifically, collagen-formulated vectors encoding PDGF-B, when delivered as subcutaneously implanted sponges, have been shown to enhance granulation tissue deposition, enhance epithelial area, and improve wound closure more effectively than aqueous formulations of the same vectors. With longer time, complete healing without excessive scar formation was achieved. In comparison, aqueous formulations allowed vector seepage and led to PDGF-induced hyperplasia in surrounding tissues but not in wound beds. In addition, repeated applications of PDGF-BB proteins were required for neotissue induction approaching equivalence to a single application of collagen-immobilized vectors. (Doukas et al., 2002, Hum. Gene Ther. 12:783-98). In the same study, Doukas et al. also showed that vectors encoding fibroblast growth factor 2 or vascular endothelial growth factor promoted primarily angiogenic responses. Similar improvements were observed in dermal ulcer wounds in the ears of young adult New Zealand white rabbits with collagen embedded PDGF-B or PDGF-A DNA plasmids (Tyrone et al., 2000, J. Surg. Res. 93:230-6); in soft tissue repair by enhancing de novo tissue formation (Chandler et al., 2000, Mol. Ther. 2:153-60).

Other materials may also be used as sustained release matrices for delivering vectors encoding PDGF genes. For example, matrices of poly(lactideco-glycolide) (PLG) were loaded with plasmids and shown to release the plasmids over a period ranging from days to months in vitro, and led to the transfection of large numbers of cells. In vivo delivery enhanced matrix deposition and blood vessel formation in the developing tissue (Shea et al., 1999, Nat. Biotechnol. 17:551-4).

Another method of gene delivery uses fusogenic virosomes. This approach combines some of the advantages of viral delivery vectors with the safety and ‘simplicity’ of the liposome to produce fusogenic virosomes (Dzau et al., 1996, Fusigenic viral liposome for gene therapy in cardiovascular diseases. Proc Natl. Acad. Sci. USA 93:11421-25). Virosomes have been engineered by complexing the membrane fusion proteins of hemagglutinating virus of Japan (HVJ, which is also known as Sendai virus) with either liposomes that already encapsulate plasmid DNA or oligodeoxynucleotides (ODN) for antisense applications. The inherent ability of the viral proteins in virosomes to cause fusion with cell membranes means that these hybrid vectors can be very efficient at introducing their nucleic acid to the target cell, resulting in good gene expression. Each viral vector has a limit on the size of transgene that can be incorporated into its genome; no such limit exists for virosome or liposome technology. Genes of up to 100 kilobase pairs have been delivered by fusogenic virosomes to cells both ex vivo and in vivo.

A further embodiment of the invention utilizes DNA-ligand conjugates for delivery of genes encoding the PDGF-polypeptides. DNA-ligand conjugates have two main components: a DNA-binding domain and a ligand for cell-surface receptors. The transgene can therefore be guided specifically to the target cell, where it is internalized via receptor-mediated endocytosis. Once the DNA-ligand complex is in the endocytic pathway, the conjugate is likely to be destroyed when the endosome fuses with a lysosome. To avoid this, an adenovirus-derived domain may be incorporated into the cell-surface receptor part of the ligand (Curiel et al, 1992, High-efficiency gene transfer mediated by adenovirus coupled to DNA-polylysine complexes, Hum. Gene Ther. 3:147-154). The conjugates then have the same specificity as adenoviruses, binding to a wide host-cell range; they also possess an adenovirus characteristic that allows the conjugate to leave the endosome and enter the cytoplasm (by a process known as endosomolysis) before the endosome is destroyed by a lysosome.

According to another embodiment of the invention, suitable host cells may be transformed with polynucleotides, preferably vectors, more preferably viral vectors, encoding the PDGF-D polypeptides of the invention, and the host cells expressing the PDGF-D polypeptides may be introduced to a host animal in need of wound healing or other treatment. Many methods of in vitro cell transformation are known and well established in the art, including CaPO₄ transfection, which is a chemical method that has been successfully used by molecular biologists for many years to introduce transgenes into cells in vitro with a relatively good efficiency (10%). Mathisen et al. showed that autoreactive memory Th2 T cells can be genetically modified so that upon engagement of self antigen they produce regenerative growth factors such as PDGF-A capable of mediating tissue repair during autoimmune disease (Mathisen et al., 1999, J. Autoimmun. 13:31-8.

Where PDGF-D is to be used for therapeutic purposes, the dose(s) and route of administration will depend upon the nature of the patient and condition to be treated, and will be at the discretion of the attending physician or veterinarian. Suitable routes include oral, subcutaneous, intramuscular, intraperitoneal or intravenous injection, parenteral, topical application, implants etc. Topical application of PDGF-D may be used in a manner analogous to VEGF. When used for stabilizing angiogenesis, an effective amount of the truncated active form of PDGF-D is administered to an organism in need thereof in a dose between about 0.1 and 1000 μg/kg body weight.

The PDGF-D may be employed in combination with a suitable pharmaceutical carrier. The resulting compositions comprise a therapeutically effective amount of PDGF-D and a pharmaceutically acceptable non-toxic salt thereof, and a pharmaceutically acceptable solid or liquid carrier or adjuvant. Examples of such a carrier or adjuvant include, but are not limited to, saline, buffered saline, Ringer's solution, mineral oil, talc, corn starch, gelatin, lactose, sucrose, microcrystalline cellulose, kaolin, mannitol, dicalcium phosphate, sodium chloride, alginic acid, dextrose, water, glycerol, ethanol, thickeners, stabilizers, suspending agents and combinations thereof. Such compositions may be in the form of solutions, suspensions, tablets, capsules, creams, salves, elixirs, syrups, wafers, ointments or other conventional forms. The formulation should be constituted to suit the mode of administration. Compositions which comprise PDGF-D may optionally further comprise one or more of PDGF-A, PDGF-B, PDGF-C, VEGF, VEGF-B, VEGF-C, VEGF-D, VEGF-E, PIGF and/or heparin. Compositions comprising PDGF-D will contain from about 0.1% to 90% by weight of the active compound(s), and most generally from about 10% to 30%.

For intramuscular preparations, a sterile formulation, preferably a suitable soluble salt form of the truncated active form of PDGF-D, such as hydrochloride salt, can be dissolved and administered in a pharmaceutical diluent such as pyrogen-free water (distilled), physiological saline or 5% glucose solution. A suitable insoluble form of the compound may be prepared and administered as a suspension in an aqueous base or a pharmaceutically acceptable oil base, e.g. an ester of a long chain fatty acid such as ethyl oleate.

In another aspect, the invention relates to use of a protein dimer comprising the PDGF-D polypeptide, particularly a disulfide-linked dimer. The protein dimers of the invention include both homodimers of PDGF-D polypeptide and heterodimers of PDGF-D and VEGF, VEGF-B, VEGF-C, VEGF-D, VEGF-E, PIGF, PDGF-A, PDGF-B or PDGF-C.

Another aspect of the invention relates to the discovery that the full length PDGF-D protein is likely to be a latent growth factor that needs to be activated by proteolytic processing to release an active PDGF/VEGF homology domain. A putative proteolytic site is found in residues 254-257 in the full length protein, residues -RKSK- (SEQ ID NO:5). This is a dibasic motif. The -RKSK (SEQ ID NO:5) putative proteolytic site is also found in PDGF-A, PDGF-B, VEGF-C and VEGF-D. In these four proteins, the putative proteolytic site is also found just before the minimal domain for the PDGF/VEGF homology domain. Together these facts indicate that this is the proteolytic site.

Preferred proteases include, but are not limited, to plasmin, Factor X and enterokinase. The N-terminal CUB domain may function as an inhibitory domain which might be used to keep PDGF-D in a latent form in some extracellular compartment and which is removed by limited proteolysis when PDGF-D is needed.

According to this aspect of the invention, a method is provided for producing an activated truncated form of PDGF-D or for regulating receptor binding specificity of PDGF-D. These methods comprise the steps of expressing an expression vector comprising a polynucleotide encoding a polypeptide having the biological activity of PDGF-D and supplying a proteolytic amount of at least one enzyme for processing the expressed polypeptide to generate the activated truncated form of PDGF-D.

This aspect also includes a method for selectively activating a polypeptide having a growth factor activity. This method comprises the step expressing an expression vector comprising a polynucleotide encoding a polypeptide having a growth factor activity, a CUB domain and a proteolytic site between the polypeptide and the CUB domain, and supplying a proteolytic amount of at least one enzyme for processing the expressed polypeptide to generate the activated polypeptide having a growth factor activity.

Also this aspect includes use of an isolated dimer comprising an activated monomer of PDGF-D and an activated monomer of VEGF, VEGF-B, VEGF-C, VEGF-D, VEGF-E, PDGF-D, PDGF-A, PDGF-B, PDGF-C or PIGF linked to a CUB domain, or alternatively, an activated monomer of VEGF, VEGF-B, VEGF-C, VEGF-D, PDGF-D, PDGF-A, PDGF-B or PIGF and an activated monomer of PDGF-D linked to a CUB domain. The isolated dimer may or may not include a proteolytic site between the activated monomer and the CUB domain.

It will be clearly understood that the PDGF-D polypeptides used in the invention may be prepared by synthetic means or by recombinant means, or may be purified from natural sources.

It will be clearly understood that for the purposes of this specification the word “comprising” means “including but not limited to.” The corresponding meaning applies to the word “comprises.”

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 (SEQ ID NO:2) shows the complete 370 ammo acid sequence of full-length human PDGF-D,

FIG. 2 (SEQ ID NO:1) shows the complete (1116 bp) nucleotide sequence of the cDNA which encodes hPDGF-D (SEQ ID NO: 2);

FIG. 3 shows the amino acid sequence of an active 200 amino acid hPDGF-D fragment (SEQ ID NO:3).

FIG. 4 shows the amino acid sequence of a 322 amino acid active hPDGF-D fragment (SEQ ID NO:4);

FIG. 5 shows an amino acid sequence alignment of the hPDGF-D with hPDGF-C (SEQ ID NOs:2 and 6, respectively);

FIG. 6 shows an amino acid sequence alignment of the CUB domain present in hPDGF-D (SEQ ID NO:7) and other CUB domains present in human bone morphogenic protein-1 (hBMP-1,3 CUB domains CUB1-3) (SEQ ID NOs:8-10, respectively) and in human neuropilin-1 (2 CUB domains) (SEQ ID NOs:11-12, respectively);

FIG. 7A shows a schematic representation of the PDGF-D sequence;

FIG. 7B shows a schematic representation of the PDGF-D sequence variant, which corresponds to FIG. 7A but for 6 missing amino acid residues;

FIG. 7C shows a schematic representation of the PDGF-D sequence variant, which corresponds to FIG. 7A but for 6 missing amino acid residues and the loss of the PDGF homology domain in this sequence variant.

FIG. 8 shows the amino acid sequences of a known VEGF-E sequence from the ORF Virus (SEQ ID NO: 15), GenBank. Accession No. AAO31702 or AF106020.

FIG. 9 shows an SDS-PAGE analysis under reducing conditions of human PDGF-DD formed from the core domain of factor Xa-digested mutant full-length form of PDGF-D;

FIG. 10 shows the in vivo angiogenic activity of human PDGF-DD and other PDGF isoforms in the mouse cornea pocket assay. The arrows in the figures point to where PDGF protein-containing beads were implanted;

FIG. 11 is a schematic diagram showing a KI4-PDGF-D construct;

FIG. 12 shows a comparison of PDGF-D expression between K14-PDGF-D transgenic mouse (TG) and wild-type mouse (wt). Paraffin embedded mouse skin samples were stained with anti-PDGF-D. For experimental details, see Uutela et al., 2001, “Chromosomal location, exon structure and vascular expression patterns of the human PDGF-C and PDGF-D genes,” Circulation 103:2242-2247;

FIGS. 13A-F show the KI4-PDGF-D transgene, its mRNA expression, expression of the transgene in the skin, and analysis of the phenotype in the dermis of transgenic mice;

FIGS. 14A and B show a schematic presentation of an AAV-PDGF-D construct and an in vitro expression analysis of AAV infected HeLa cells, and

FIGS. 15A-J show that AAV-PDGF-D infection of mouse ears stabilizes and reduces leakage of blood vessels induced by VEGF-E.

FIG. 16 shows that transgenic mice expressing both PDGF-D and VEGF-E had significantly less blood vessel leakage as compared to transgenic mice expressing VEGF-E alone.

DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS

The present invention discloses a method of modulating, regulating and/or stabilizing angiogenesis in a mammal in need thereof, in which the PDGF-D level or activity or both in the mammal are modulated, preferably increased. In preferred embodiments, an active PDGF-D polypeptide in suitable amounts is directly administered to the mammal, or a polynucleotide encoding an active PDGF-D polypeptide is administered to the mammal, preferably at a location where angiogenesis modulating or stabilization is desired. Alternatively, endogenous expression of PDGF-D may be manipulated, either by increasing the expression level, or decreasing the degradation or clearing of expressed endogenous PDGF-D.

In a preferred embodiment, the PDGF-D is advantageously coadministered with an angiogenic growth factor, such as a member of the VEGF/PDGF family of growth factors, in particular VEGF-E.

The claimed method inhibits leakage of blood vessels and is useful, inter alia, for treatment of edemas. The known effects of increasing angiogenesis by, e.g. VEGF-E, and the angiogenesis stabilizing effects of PDGF-D; when combined according to the methods of the present invention, can be used for promoting wound healing as well as for other clinical treatment methods where angiogenesis promotion is desired.

Construction of PDGF-D Variants, Derivatives and Analogues

PDGF-D is a member of the PDGF family of growth factors which exhibits a high degree of homology to the other members of the PDGF family. PDGF-D contains seven conserved cysteine residues which are characteristic of this family of growth factors. These conserved cysteine residues form intra-chain disulfide bonds which produce the cysteine knot structure, and inter-chain disulfide bonds that form the protein dimers which are characteristic of members of the PDGF family of growth factors. PDGF-D interacts with a protein tyrosine kinase growth factor receptor.

In contrast to proteins where little or nothing is known about the protein structure and active sites needed for receptor binding and consequent activity, the design of active mutants of PDGF-D is greatly facilitated by the fact that a great deal is known about the active sites and important amino acids of the members of the PDGF family of growth factors.

Published articles elucidating the structure/activity relationships of members of the PDGF family of growth factors include for PDGF: Oestman et al., 1991, J. Biol. Chem., 266:10073-10077; Andersson et al., 1992, J. Biol. Chem., 267:11260-1266; Oefner et al., 1992, EMBO J., 11:3921-3926; Flemming et al., 1993, Molecular and Cell Biol., 13:4066-4076 and Andersson et al., 1995, Growth Factors, 12:159-164; and for VEGF: Kim et al., 1992, Growth Factors, 7:53-64, Pötgens et al., 1994, J. Biol. Chem., 269:32879-32885 and Claffey et al., 1995, Biochem. Biophys. Acta, 1246:1-9. From these publications it is apparent that because of the eight conserved cysteine residues, the members of the PDGF family of growth factors exhibit a characteristic knotted folding structure and dimerization, which result in formation of three exposed loop regions at each end of the dimerized molecule, at which the active receptor binding sites can be expected to be located.

Based on this information, a person skilled in the biotechnology arts can design PDGF-D mutants with a very high probability of retaining PDGF-D activity by conserving the eight cysteine residues responsible for the knotted folding arrangement and for dimerization, and also by conserving, or making only conservative amino acid substitutions in the likely receptor sequences in the loop 1, loop 2 and loop 3 region of the protein structure.

As used herein, the term “conservative substitution” denotes the replacement of an amino acid residue by another, biologically similar residue. Examples of conservative substitutions include the substitution of one hydrophobic residue such as isoleucine, valine, leucine, alanine, cysteine, glycine, phenylalanine, proline, tryptophan, tyrosine, norleucine or methionine for another, or the substitution of one polar residue for another, such as the substitution of arginine for lysine, glutamic acid for aspartic acid, or glutamine for asparagine, and the like. Neutral hydrophilic amino acids which can be substituted for one another include asparagine, glutamine, serine and threonine. The term “conservative substitution” also includes the use of a substituted amino acid in place of an unsubstituted parent amino acid.

As such, it should be understood that in the context of the present invention, a conservative substitution is recognized in the art as a substitution of one amino acid for another amino acid that has similar properties. Exemplary conservative substitutions are set out In the following Table A from WO 97/09433.

TABLE A Conservative Substitutions I SIDE CHAIN CHARACTERISTIC Aliphatic AMINO ACID Non-polar G A P I L V Polar-uncharged C S T M N Q Polar-charged D E K R Aromatic H F W Y Other N Q D E

Alternatively, conservative amino acids can be grouped as described in Lehninger, Biochemistry, Second Edition; Worth Publishers, Inc. NY:NY (1975), pp. 71-77 as set out in the following Table B.

TABLE B Conservative Substitutions II SIDE CHAIN CHARACTERISTIC AMINO ACID Non-polar (hydrophobic) A. Aliphatic: A L I V P B. Aromatic: F W C. Sulfur-containing: M D. Borderline G Uncharged-polar A. Hydroxyl: S T Y B. Amides: N Q C. Sulfhydryl: C D. Borderline: G Positively Charged (Basic) K R H Negatively Charged (Acidic) D E

Exemplary conservative substitutions are set out in the following Table C.

TABLE C Conservative Substitutions III Original Residue Exemplary Substitution Ala (A) Val, Leu, Ile Arg (R) Lys, Gln, Asn Asn (N) Gln, His, Lys, Arg Asp (D) Glu Cys (C) Ser Gln (Q) Asn Glu (E) Asp His (H) Asn, Gln, Lys, Arg Ile (I) Leu, Val, Met, Ala, Phe, Leu (L) Ile, Val, Met, Ala, Phe Lys (K) Arg, Gln, Asn Met (M) Leu, Phe, Ile Phe (F) Leu, Val, Ile, Ala Pro (P) Gly Ser (S) Thr Thr (T) Ser Trp (W) Tyr, Phe Tyr (Y) Trp, Phe, Thr, Ser Val (V) Ile, Leu, Met, Phe, Ala

If desired, the peptides of the invention can be modified, for instance, by glycosylation, amidation, carboxylation, or phosphorylation, or by the creation of acid addition salts, amides, esters, in particular C-terminal esters, and N-acyl derivatives of the peptides of the invention. The peptides also can be modified to create peptide derivatives by forming covalent or noncovalent complexes with other moieties. Covalently-bound complexes can be prepared by linking the chemical moieties to functional groups on the side chains of amino acids comprising the peptides, or at the N- or C-terminus.

The formation of desired mutations at specifically targeted sites in a protein structure is considered to be a standard technique in the arsenal of the protein chemist (Kunkel et al., 1987, Methods in Enzymol. 154:367-382). Examples of such site-directed mutagenesis with VEGF can be found in Pötgens et al., 1994, J. Biol. Chem. 269:32879-32885 and Claffey et al., 1995, Biochem. Biophys. Acta, 1246:1-9. Indeed, site-directed mutagenesis is so common that kits are commercially available to facilitate such procedures (e.g. Promega 1994-1995 Catalog., Pages 142-145).

PDGF-D derivatives, variants and analogs of the present invention further include polypeptides that are at least 70% or at least 80% identical to SEQ ID NO:2, SEQ ID NO: 3 (the 200 amino acids set out in FIG. 3) or SEQ ID NO: 4 (the 322 amino acid sequence set out in FIG. 4 (SEQ ID NO:4), or amino acids 254-370 of FIG. 1 which is the PVDH domain.

In this regard, polypeptides at least 90% identical to the same are particularly preferred, and among these particularly preferred polynucleotides, those with at least 95% are especially preferred. Furthermore, those with at least 97% are highly preferred among those with at least 95%, and among these those with at least 98% and at least 99% are particularly highly preferred, with at least 99% being the more preferred.

PDGF-D derivatives, variants and analogs of the present invention further include polynucleotides encoding the polypeptides described above.

The activity, especially the angiogenesis modulating, regulating and/or stabilizing activity, PDGF-D mutants can be readily confirmed by well-established routine screening procedures using methods which are well known in the art.

FIG. 1 shows the amino acid sequence of full-length HPDGF-D containing 370 amino acid residues (SEQ ID NO:2). FIG. 2 (SEQ ID NO:1) shows the 1116 bp polynucleotide sequence of a cDNA encoding full-length HPDGF-D.

PDGF-D has a two-domain structure with a N-terminal CUB domain (residues 67-167, discussed below) and a C-terminal PDGF/VEGF homology domain. The homology domain, alternatively known as the core domain, can be as long as residues 254-370, or as short as residues 272-362, and includes any intermediate fragment in between. The overall ammo acid sequence identity between PDGF-C (SEQ ID NO:6) and PDGF-D (SEQ ID NO:2) is approximately 43% (FIG. 5). The similarities are highest in the distinct protein domains while the N-terminal region, including the hydrophobic signal sequence, and the hinge region between the two domains display lower identities. A putative signal peptidase cleavage site was identified between residues 22-23. Cleavage results in a protein of 348 residues with a calculated molecular mass (M_(r)) of 44,000. A single putative site for N-linked glycosylation was identified in the core domain of PDGF-D (residues 276-278).

With two exceptions, PDGF-D has the expected pattern of invariant cysteine residues, involved in inter- and intra-disulfide bonding, a hallmark of members of this family. The first exception occurs between cysteine 3 and 4. Normally these two cysteines are spaced by 2 residues. However, similar to PDGF-C, PDGF-D has an unique insertion of three additional amino acids residues, NCG. In total, ten cysteine residues reside in the core domain, including the extreme C-terminal region, suggesting a unique arrangement of the cysteines in the disulfide-bonded PDGF-D dimer. The second exception is that the invariant fifth cysteine found in the other members of the PDGF/VEGF family is not conserved in PDGF-D. This feature is unique to PDGF-D.

The N-terminal region of the partial PDGF-D amino acid sequence of FIG. 6 (residues 53-170 of SEQ ID NO:2) has a second distinct protein domain which is referred to as a CUB domain (Bork and Beckmann, 1993, J. Mol. Biol. 231:539-545). This domain of about 115 amino acids was originally identified in complement factors C1r/C1s, but has recently been identified in several other extracellular proteins including signaling molecules such as bone morphogenic protein 1 (BMP-1) (Wozney et al, 1988, Science, 242:1528-1534) as well as in several receptor molecules such as neuropilin-1 (NP-1) (Soker et al., 1998, Cell 92:735-745). The functional roles of CUB domains are not clear but they may participate in protein-protein interactions or in interactions with carbohydrates including heparin sulfate proteoglycans. These interactions may playa role in the proteolytic activation of PDGF-D.

PDGF-DD is a PDGFR-beta-specific agonist. Proteolytic processing of PDGF-DD releases the core domains from the N-terminal CUB domains which is necessary for unmasking the receptor-binding epitopes of the core domain similar to the situation for PDGF-CC.

Murine PDGF-D sequences have been determined. A second mouse clone was almost identical to an earlier mouse sequence identified, however, it lacked six amino acid residues (aa 42-47) from the region between the signal sequence and the CUB domain.

A third mouse clone was also obtained which comprised of part of the earlier mouse sequence, lacking amino acids 42-47 as in the second clone, and also lacking the PDGF-homology domain. The similarities and differences between regions of the three clones are depicted in FIG. 7.

The surprising results show that at least two alternatively spliced versions of the PDGF-D gene are transcribed into polyadenylated RNA. The variant transcript structures suggest an alternative splice acceptor site is used in exon two, producing a variant protein lacking six amino acid residues (ESNHLT).

In addition to lacking the above noted six amino acid residues, the third clone also lacks the PDGF-homology domain. This is because of the skipping of exon six and the resulting frame shift. This ends the open reading frame in a stop codon after four additional amino acid residues (GIEV). As shown in detail in FIG. 8, this splice variant only contains the amino terminal CUB domain and could potentially provide an inhibitor of PDGF-D functions. The potential inhibition function is because the activation of full-length PDGF-D binding to the PDGFR-D requires proteolytic removal of the CUB domain.

EXAMPLES Example 1 Generation of Recombinant Human PDGF-DD Core Domain

The process as described (Bergsten et al., 2001, Nat. Cell Biol. 3:512-516) was followed to generate recombinant human PDGF-DD core domain. Human PDGF-DD was expressed as a mutant full-length form containing a factor Xa protease cleavage site. Amino acids 251-258 were replaced with 2 tandem factor Xa cleavage sites of Ile Glu Gly Arg residues 1-4 of SEQ ID NO: 5 (i.e. Ile Glu Gly Arg Ile Glu Gly Arg; SEQ ID NO: 5) that allowed the generation of the active C-terminal fragment of the protein (PDGF-homology domain) upon cleavage with factor Xa. The recombinant protein has an extreme C-terminal His₆-tag (SEQ ID NO: 16) to allow its purification on a nickel-containing resin. Following purification, the protein solution was dialyzed against 0.1M acetic acid and lyophilized. SDS-PAGE analysis under reducing conditions on the purified protein revealed that it migrated as a homogenous 21 kDa species (see FIG. 9). The purified protein was lyophilized for storage.

Example 2 Comparison of Angiogenic Activities of the Human PDGF-DD Core Domain with Other PDGF Isoforms

The mouse corneal micropocket assay was performed according to procedures described in Cao et al., 1998, Proc Nat'l. Acad. Sci. USA 95:14389-94, Cao et al., 1999, Nature 398:381. Specifically, lyophilized proteins were dissolved in phosphate buffer solutions (PBS) and used to make protein bound polymer beads, as described.

The beads were then implanted in mouse cornea. Male 5-6 week-old C57BI6/J mice were acclimated and caged in groups of six or less. Animals were anaesthetized by injection of a mixture of dormicum and hypnorm (1:1) before all procedures. Corneal micropockets were created with a modified von Graefe cataract knife in both eyes of each male 5-6-week-old C57BI6/J mouse. A micropellet (0.35×0.35 mm) of sucrose aluminum sulfate (Bukh Meditec, Copenhagen, Denmark) coated with slow-release hydron polymer type NCC (IFN Sciences, New Brunswick, N.J.) containing various amounts of homodimers of truncated PDGF-DD was surgically implanted into each corneal pocket.

For comparison purposes corresponding amounts of PDGF-AA, PDGF-AB, PDGF-BB, and PDGF-CC were similarly implanted into corneal pockets of test mice. In each case, the pellet was positioned 0.6-0.8 mm from the corneal limbus. After implantation, erythromycin/ophthalmic ointment was applied to each eye.

On day 5 after growth factor implantation, animals were sacrificed with a lethal dose of CO₂, and corneal neovascularization was measured and photographed with a slit-lamp stereomicroscope. In FIGS. 10A-E, arrows point to the implanted pellets. Vessel length and clock hours of circumferential neovascularization were measured. Quantitation of corneal neovascularization is presented as maximal vessel length (FIG. 10F), clock hours of circumferential neovascularization (FIG. 10G), and area of neovascularization (FIG. 10H). Graphs represent mean values (A SEM) of 11-16 eyes (6-8 mice) in each group.

The corneal angiogenesis model is one of the most rigorous mammalian angiogenesis models that requires a putative compound to be sufficiently potent in order to induce neovascularization in the corneal avascular tissue. Potent angiogenic factors including FGF-2 and VEGF have profound effects in this system.

The results are shown in FIG. 10. The assays were done using PDGF-AA (FIG. 10A), PDGF-AB (FIG. 10B), PDGF-BB (FIG. 10C), PDGF-CC (FIG. 10D), and PDGF-DD (FIG. 10C). FIGS. 10F-H show the quantitative analysis of vessel length, clock hours, and vessel areas (means±SD, n=4-6).

The overall angiogenic response induced by PDGF-DD was similar to that induced by other PDGF isoforms. The results again clearly demonstrate that the truncated PDGF-D homodimer exhibits marked angiogenic activity in vivo. In light of the foregoing test results, which demonstrate the in vivo angiogenesis inducing activity of PDGF-DD, treatments with PDGF-DD alone, or in combination with other angiogenic factors such as VEGF family members and FGFs, provide an attractive approach for therapeutic angiogenesis of ischemic heart, brain and limb disorders.

Example 3 Generation and Analysis of KI4-PDGF-D Transgenic Mice

Human PDGF-D cDNA (bp 176-1285; GenBank seq. number: AF336376) was inserted into the Bam HI site of the K14 promoter expression vector [Vassar et al., 1989, Proc. Natl. Acad. Sci. USA 86:1563-1567]. This directs expression of the gene to the basal epithelial cells of the skin of transgenic animals (Jeltsch et al. 1997 Hyperplasia of lymphatic vessels in VEGF-C transgenic mice. Science 276:1423-1425). FIG. 13A shows a schematic diagram of the resulting KI4-PDGF-D construct. The construct was digested with EcoRI and SphI and the expression cassette was purified. A 5 ng/μl solution of the DNA was injected into fertilized eggs of the FVB-strain of mice and the resulting transgenic mice were maintained in this strain. To analyze the transgene expression, PDGF mRNA expression in the skin of transgenic and wild type littermate mice was studied. Tissues were snap-frozen in liquid nitrogen and homogenized with a dismembrator. Total RNA was extracted with the RNEasy Kit (QIAGEN GmbH). 10-20 μg g of total RNA was electrophoresed in 1% agarose and transferred to a nylon membrane (Nytran, Schleicher & Schuell), which was then hybridized with a human PDGF-D probe (bp 119 to 1268) and subjected to autoradiography. Protein expression was verified by immunohistochemistry using anti-PDGF-D antibodies [Uutela et al., 2001, Circulation 103:2242-2247]. Two transgenic lines were used for the analysis.

PDGF-D expression was detected in the skin of the transgenic, but not control littermate mice by Northern hybridization and immunohistochemistry. FIG. 13B is a Northern blot of skin total RNA hybridized with radioactive PDGF-D probe showing the mRNA product of the transgene construct. Equal loading of the first two lanes was confirmed by ethidium bromide staining of RNA. FIGS. 13C through 31F show immunostaining of the skin. Using paraffin-embedded mouse skin samples, an anti-PDGF-D antibody was shown to stain the basal keratinocytes in K14-PDGFD skin (FIG. 13C, arrowheads) but not in wild type littermate skin (FIG. 13D). A Rat anti-mouse monoclonal antibody which detects macrophages (Serotec) was used to stain for F4/80 which detects macrophages. Very strong staining in the transgenic mouse skin (FIG. 13E, arrowheads) was seen when compared to wild type littermate skin (FIG. 13F).

Example 4 Generation of AAV Expression Vectors

In order to analyze the effects of PDGF-D expression in adult skin and muscle, AAV vectors encoding the full-length PDGF-D (DFL) or the activated form (ΔN) lacking the CUB domain were generated and tested in vitro. AAV encoding HSA was used as a control. VEGF-E was also cloned into AAV. FIG. 14B shows an in vitro expression analysis of AAV infected HeLa cells. The PDGFs were precipitated with PDGFR-.B-Ig and VEGF-E with VEGFR-2-Ig.

The full length VEGF-E (bp 1-399, GenBank seq. AF106020), the full length PDGF-D (PDGF-DFL), and a short form (PDGF-DAN, bp 917-1285) as well as human serum albumin (HSA, bp 112-1866, GenBank seq. NM_(—)000477) cDNAs were cloned as blunt-end fragments into the MluI site of the psub-CMV-WPRE plasmid [Paterna et al., 2000, Gene Ther. 7:1304-1311]. FIG. 14A is a schematic presentation of the AAV-PDGF-D constructs. The human PDGF-DFL, PDGF-DΔN, VEGF-E and HSA cDNAs are driven by the CMV promoter and early enhancer (CMV), promoted by the Woodchuck posttranscriptional enhancer-element (WPRE). pA is the SV40 polyadenylation signal. The recombinant AAVs were produced as described in Karkkainen et al., 2001, A model for gene therapy of human hereditary lymphedema, Proc. Nat'l. Acad. Sci. USA 98:12677-12682. 50 μl of purified AAV (5×10¹¹ genomic particles/ml) was injected into mouse ear or gastrognemius muscle and four weeks later the mice were sacrificed and the tissues analyzed.

To construct a VEGFR-2/IgG expression plasmid, the first three Ig homology domains of the extracellular part of VEGFR-2 were amplified by PCR using primers 5′-GCGGATCCTTGCCTAGTGTTTCTCTTGATC-3′ (SEQ ID NO:13) and 5′-CCAGTCACCTGCTCCGGATCTTCATGGACCCTGACAAATG-3′ (SEQ ID NO:14) and cloned into the Signal pIgplus vector (Ingenius). The resulting plasmid was cut with BamHI and KpnI, treated with T4 polymerase and back-ligated. The generation of stable Drosophila S2 cells and purification of the VEGFR-2-Ig fusion proteins was carried out as described by Makinen et al., 2001, Inhibition of lymphangiogenesis with resulting lymphedema in transgenic mice expressing soluble VEGF receptor-3, Nat. Med. 7:199-205.

HeLa cells were infected with 2 μl purified AAV (5×10¹¹ genomic particles/ml) in 5 ml DMEM supplemented with 2% fetal bovine serum and glutamine overnight, after which the cells were washed and cultured for further 24 hours in DMEM supplemented with 10% fetal bovine serum and glutamine. The cells were metabolically labeled in methionine and cysteine free MEM supplemented with 100 μCi/ml [³⁵S] methionine and [³⁵S] cysteine (Redivue ProMix; Amersham Pharmacia Biotech). Immunoprecipitation of metabolically 35S-labeled PDGF-D was carried out by using PDGFR-α-Ig or PDGFR-β-Ig (R&D), and VEGF-E was precipitated by a VEGF receptor 2-Ig. The complexes were adsorbed to protein A-sepharose (pharmacia), washed twice in 0.5% BSA, 0.02% Tween 20 in PBS, and once in PBS and analyzed in a 12.5% SDS-PAGE under reducing conditions.

Example 5 Stabilization of VEGF-E Induced Blood Vessels by PDGF-D

PDGF-B has been implicated in the stabilization of blood vessels during angiogenesis [Saharinen et al., 2003, Double target for tumor mass destruction. J. Clin. Invest. 111:1277-1280]. To investigate the possible contribution to angiogenic responses, AAV-PDGF-D was tested, alone in combination with AAV producing the angiogenic factor VEGF-E, in the ears of 46 week old mice. In addition, transgenic mice expressing K14-PDGF-D or K14-VEGF-E were also compared with transgenic mice that express both K14-PDGFD and K14-VEGF-E.

a. AAV Infection Experiments

AAV-PDGF-D and AAV-VEGF-E, alone or in combination, were used to infect ears of 4-6 weeks mice, and the blo9d vessels of the ears were examined using the FITC-Dextran staining as described by Fukumura et al., 1995, Tumor necrosis factor a-induced leucocyte adhesion in normal and tumor vessel: effect of tumor type, transplantation site, and host strain, Cancer Res. 55:4824-4829. Briefly, mice were anesthetized and 200 μl FITC-Dextran (2000 kDa, 20 mg/ml in phosphate-buffered solution) was injected intravenously into the tail vein through a 30 G needle. The ears were monitored under a fluorescence microscope, and equal length exposed pictures were taken after 1, 2 and 4 minutes. Fluorescent microangiography was performed as described by Saaristo et al., 2002, Lymphangiogenic gene therapy with minimal blood vascular side effects, J. Exp. Med. 196:719-730.

Whole mount staining of smooth muscle actin (SMA) positive blood vessels was performed by first fixing the ears with 4% paraformaldehyde, after this, tissues were blocked in 3% milk 0.3% Triton-X in PBS overnight and Cy³ conjugated antibodies against SMA (Sigma) were applied overnight at +4° C. and viewed in a Zeiss Axioplan 2 fluorescent microscope.

AAV-VEGF-E was found to induce a strong angiogenic response detected in whole mount ears stained for the PECAM-1 and SMA. Vessels were increased in diameter (see arrowheads in FIG. 15A) in comparison to AAV-HSV (FIG. 15B). The AAV-VEGF-E infected ears stained for SMA showed a loose, irregular coating by smooth muscle cells (FIGS. 15A and 15C) in comparison with AAV-HSA infected ears. Interestingly, the ears injected with the combination of AAV-PDGF-D and AAV-VEGF-E, showed a normal tight structure of the smooth muscle layer (FIGS. 15D and 15F), similar to the AAVHSA or AAV-PDGF-D injected ears (FIGS. 15B and 15E) and the vessels had an increased diameter. When tested for vascular leakiness by injecting FITC-Dextran into the tail vein, the vessels in the ears treated with the combination of AAV-PDGF-D and AAV-VEGF-E had clearly reduced leakiness (FIG. 151) in comparison with the vessels formed in the ears injected with AAV-VEGF-E only (FIG. 15G). In contrast, the VEGF-E induced increase of blood capillaries was unaffected and AAV-PDGF-D alone did not seem to have an effect on the smooth muscle cell coating or leakiness of the vessels (FIG. 15J).

When the angiogenic effects of PDGF-D gene transduction in the ear and skeletal muscle were tested, PDGF-D alone was not angiogenic. But when PDGF-D was expressed together with VEGF-E, which has been shown to induce a strong angiogenic response [Kiba et al., 2003, VEGFR-2-specific ligand VEGF-E induces non-edematous hyper-vascularization in mice. Biochem. Biophys. Res. Commun. 301:371-377], PDGF-D was found to stabilize newly generated, enlarged and leaky vessels induced by VEGF-E alone. This effect may due to the PDGF-D induced stimulation of the proliferation and migration of smooth muscle cells (SMCs), as has been shown for coronary artery SMCs in vitro [Uutela et al., 2001, Chromosomal Location, Exon Structure and Vascular Expression Patterns of the Human PDGF-C and PDGF-D Genes. Circulation 103:2242-2247]. Consistent with such a possibility, the whole mount staining for smooth muscle actin indicated that the vessels induced by VEGF-E have an abnormally sparse SMC coating, but when combined with PDGF-D, the SMC layer seemed comparable to that in the untreated skin. This indicates that PDGF-D can play an important role in stabilizing newly formed vessels by recruiting SMCs.

b. Transgenic Mice Experiment

K14-PDGF-D transgenic mice were generated and examined as described in Example 3, supra. Transgenic mice expressing K14-VEGF-E were obtained courtesy of Shibuya and were previously published (Kiba et al., (2003) VEGFR-2-specific ligand VEGF-E induces non-edematous hyper-vascularization in mice. Biochem. Biophys. Res. Commun., 301:371-377). K14-PDGF-D mice were mated with K14-VEGF-E mice, and progeny expressing both PDGF-D and VEGF-E were selected. FITC-Dextran staining on PDGF-D, VEGF-E and PDGF-D/VEGF-E, as well as wild-type mice were performed as described above. The results are shown in FIG. 16. The results demonstrate that blood vessels in the VEGF-E transgenic mice showed significant leakage, while the PDGF-D transgenic mice were virtually indistinguishable from the wild-type mice. Significantly, in the mice expressing both VEGF-E and PDGF-D, the leakage induced by VEGF-E was reduced.

The foregoing description and examples have been set forth merely to illustrate the invention and are not intended to be limiting. Since modifications of the disclosed embodiments incorporating the spirit and substance of the invention may occur to persons skilled in the art, the invention should be construed broadly to include all variations falling within the scope of the appended claims and equivalents thereof. All references cited hereinabove and/or listed below are hereby expressly incorporated by reference. 

1. A method for modulating, regulating or stabilizing angiogenesis in a mammal in need thereof, comprising administering an amount of a polynucleotide which encodes active PDGF-D sufficient to increase the level or activity of PDGF-D in said mammal. 2-11. (canceled)
 12. The method according to claim 11, wherein the polynucleotide encodes an active PDGF-D polypeptide comprises an amino acid sequence which is at least 95% identical to SEQ ID NO: 2, SEQ ID NO: 3 or SEQ ID NO:
 4. 13. The method according to claim 11, wherein an additional polynucleotide encoding an active VEGF-E polypeptide is co-administered to the mammal.
 14. The method according to claim 13, wherein additional polynucleotide encodes an active VEGF-E polypeptide comprising an amino acid sequence which is at least 95% identical to SEQ ID NO: 15 or SEQ ID NO:
 16. 15. The method according to claim 14, wherein the polynucleotide encoding the active PDGF-D polypeptide, or the additional polynucleotide encoding the active VEGF-E polypeptide, or both, are operably linked to a suitable promoter.
 16. The method according to claim 14, wherein the promoter is a tissue specific promoter. 17-21. (canceled)
 22. The method according to claim 1, wherein the mammal is human.
 23. (canceled)
 24. The method according to claim 1, wherein the polynucleotide encoding an active PDGF-D polypeptide is an expression vector expressing the PDGF-D polypeptide.
 25. The method according to claim 24, wherein the expression vector is delivered in a cell comprising the expression vector.
 26. The method according to claim 25, wherein the cell is a cell derived from the mammal in need thereof.
 27. The method according to claim 24, wherein the vector is a viral vector selected from the group consisting of a retrovirus vector, an adenovirus vector, an adeno-associated virus vector, a vaccinia virus vector, a herpes simplex virus vector, and a chimeric viral vector.
 28. The method according to claim 1, wherein the polynucleotide encoding an active PDGF-D polypeptide is a plasmid, and wherein the plasmid is topically administered in association with one or more additional therapies for wound-healing.
 29. The method according to claim 28, wherein the additional therapy for wound-healing is artificial skin or dressing for wounds. 